UV-Light-Induced Dehydrogenative N-Acylation of Amines with 2-Nitrobenzaldehydes To Give 2-Aminobenzamides

Author:

Deng Wei1,Qiu Renhua1ORCID,Zeng Dishu1,Yang Tianbao1,Tang Niu1,Xiang Jiannan1,Yin Shuang-Feng1,Kambe Nobuaki2

Affiliation:

1. State Key Laboratory of Chemo/Biosensing and Chemometrics, Advanced Catalytic Engineering Research Center of the Ministry of Education, College of Chemistry and Chemical Engineering, Hunan University

2. The Institute of Scientific and Industrial Research, Osaka University

Abstract

AbstractA simple, mild, green, and efficient method for the synthesis of 2-aminobenzamides is highly desirable. Herein, we report the development of an efficient, one-pot strategy starting from 2-aminobenzaldehydes and amines with acetic acid in ethyl acetate/acetone using irradiation with UV light for the synthesis of 2-aminobenzamides in high yields; 32 examples proceeded successfully by this photo-induced protocol in up to 92% yield. The reaction was also readily achieved on a gram scale. The utility of the 2-aminobenzamide building block in organic synthesis was shown by their use in the preparation of quinazolinone derivatives. The method was applied to amino acid derivatives as the amine component, which smoothly gave N-(2-aminobenzoyl)acetate derivatives at room temperature. Finally, a plausible mechanism is proposed.

Funder

National Natural Science Foundation of China

High-end Foreign Experts Recruitment Plan of China

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry,Catalysis

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